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Clinical Research Associate

10 Oct 2008

An interesting opportunity has developed within a global clinical research organisation for a Senior Clinical Research Associate. They are committed to providing a high quality and service in all aspects of the projects they work on.

The Senior Clinical Research Associate will work with the Directors, Clinical Project Manager, Clinical Research Executive and other staff in primarily technical aspects of the business, but will also be involved in some business development and general office organisation tasks.

Key responsibilities:
review / preparation of draft clinical study protocols
review / preparation of draft Investigator Brochures
review of draft Case Report Forms for clinical studies
monitoring of clinical study sites as appropriate, including pre-study, initiation, monitoring and close-down meetings with clinical study investigators
identification of clinical investigators
management of the Trial Master File for clinical studies as per GCP
handling of telephone and other enquiries from study site staff and clients during a study, as appropriate
management of the reporting of adverse events, as appropriate

Qualifications:
They will have competent word processing skills (including use of the MS Office applications Word, Excel, PowerPoint and Outlook)
Have relevant experience from working as a Clinical Research Associate in a pharmaceutical or healthcare product development environment.

For further information please contact
Rowena Weighell
Email: rowena.weighell@hayspharma.com

Services advertised by Hays Pharma are those of an Agency and/or an Employment Business